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FDA 510(k)

Nouvo安全套件

K号: K232234 · 2024-03-15

决定日期2024-03-15
产品代码FOZ
咨询委员会医疗设备监管文本翻译如下: HO 请注意,由于您没有提供具体的医疗设备监管文本内容,以上仅为示例。请提供具体的文本内容以便进行准确的翻译。
决定实质等同

器械摘要

Nouvo Safety Set is the device name listed in this FDA 510(k) record. The listed applicant is Poly Medicure Limited. It received FDA 510(k) clearance on 2024-03-15 under 510(k) number K232234. The device is classified under product code FOZ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Nouvo Safety Set?

Nouvo Safety Set is a medical device that received FDA 510(k) clearance on 2024-03-15. The listed applicant is Poly Medicure Limited. The 510(k) number is K232234.

When did Nouvo Safety Set receive FDA 510(k) clearance?

Nouvo Safety Set received FDA 510(k) clearance on 2024-03-15, under 510(k) number K232234.

Who is the listed applicant for Nouvo Safety Set?

The FDA 510(k) record lists Poly Medicure Limited as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Nouvo Safety Set?

The FDA product code for Nouvo Safety Set is FOZ.

相关临床试验

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列明Poly Medicure Limited为申报人的其他记录

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相关器械(代码:FOZ)

关联记录通过名称、产品代码或其他元数据自动匹配。匹配不意味着已验证临床、科学、企业或监管关系;请查阅链接的官方来源。

官方来源

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